Peer-Reviewed Journal Details
Mandatory Fields
Buckley, DA;Loughran, G;Murphy, G;Fennelly, C;O'Connor, R
2002
February
Journal Of Clinical Pathology-Molecular Pathology
Identification of an IGF-1R kinase regulatory phosphatase using the fission yeast Schizosaccharomyces pombe and a GFP tagged IGF-1R in mammalian cells
Validated
WOS: 19 ()
Optional Fields
GROWTH-FACTOR RECEPTOR FACTOR-I RECEPTOR PROTEIN TRANSFORMATION LACKING
55
46
54
Aims: To study the regulation of type 1 insulin like growth factor receptor (IGF-1 R) tyrosine kinase activity using the fission yeast Schizosaccharomyces pombe and a green fluorescent protein (GFP) tagged, full length IGF-1 R. Methods: The beta chain of the IGF-1 R (betawt) was expressed under inducible conditions in the fission yeast S pombe. Western blot analysis with antiphosphotyrosine antibodies was used to assess the kinase activity of betawt. A GFP tagged IGF-1 R (GFP-IGF-1 R) was constructed to study the tyrosine kinase activity of the full length IGF-1 R. The signalling capabilities of GFP-IGF-1 R in response to IGF-1 stimulation were investigated in transiently transfected fibroblasts. Immunofluorescent staining for cellular phosphotyrosine content was used to assess the localisation and tyrosine kinase activity of GFP-IGF-1 R. Results: The betawt protein displayed functional tyrosine kinase activity in S pombe and phosphorylated endogenous yeast proteins. In response to IGF-1 stimulation, the GFP-IGF-1 R became autophosphorylated and also activated the phosphatidylinositol 3-kinase and mitogen activated protein kinase pathways. Tyrosine phosphorylation and kinase activity of the GFP-IGF-1 R could be visualised by immunofluorescence with antiphosphotyrosine antibodies. Coexpression of a mammalian tyrosine phosphatase PTP 1 B with betawt completely inhibited this tyrosine kinase activity in yeast and also reduced the tyrosine phosphorylation in COS cells transfected with the GFP-IGF-1 R. Conclusions: Schizosaccharomyces pombe can be used to analyse the tyrosine kinase activity of the IGF-1 R beta chain and its regulation by tyrosine phosphatases. In addition, the regulation of IGF-1 R tyrosine kinase activity can be studied using a GFP tagged IGF-1 R. Using both of these methods, IGF-1 R kinase activity was shown to be inhibited by the protein tyrosine phosphatase, PTP 1 B.
LONDON
1366-8714
Grant Details